# FDA recall Z-0532-2024

> **Encore Medical, LP** · Class II · device recall initiated 2023-09-06.

## Product

RSP Glenoid Baseplate, 30mm P2 Porous Coated REF 508-32-204. DJO Surgical shoulder device.

## Reason for recall

Coating hex did not engage with the Straight Mod Hexdriver or with the Hex Head Screw Driver

## Distribution

U.S.: AZ, CA, FL, IN, KS, KY, ME, MN, MS, NJ, OH, Puerto Rico, RI, SC, TN, TX, VA, and WA  O.U.S.: None

## Key facts

- **Recall number:** Z-0532-2024
- **Recalling firm:** Encore Medical, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-09-06
- **Report date:** 2023-12-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Austin, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0532-2024

## Citation

> AI Analytics. FDA recall Z-0532-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-0532-2024. Source: US FDA. Licensed CC0.

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